Vianna E N, Costa J O, Santos C K S, Cury M C, Silva E F, Costa A O, Gomes M A
Departamento de Parasitologia, ICB, Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627-31270-901, Belo Horizonte, Minas Gerais, Brazil.
Parasitology. 2009 Jun;136(7):765-9. doi: 10.1017/S0031182009006167.
Since it is known that Entamoeba dispar is non-pathogenic and morphologically similar to E. histolytica, there are many targets used in PCR for differentiating these species. However, obtaining high quality DNA from fecal samples is fundamental for PCR. Most methods are laborious or use kits that make diagnosis expensive. In the present work, a new simple, fast and cheap technique of DNA extraction from fecal samples was combined with a PCR for an episomal target in order to identify E. histolytica and E. dispar in feces.
由于已知溶组织内阿米巴非致病性且在形态上与溶组织内阿米巴相似,因此在聚合酶链反应(PCR)中有许多用于区分这些物种的靶点。然而,从粪便样本中获取高质量的DNA是进行PCR的基础。大多数方法都很繁琐,或者使用的试剂盒使诊断成本很高。在本研究中,一种从粪便样本中提取DNA的新的简单、快速且廉价的技术与针对附加型靶点的PCR相结合,以鉴定粪便中的溶组织内阿米巴和溶组织内阿米巴。